{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Research Triangle Park",
      "state": "NC",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "77230",
      "recalling_firm": "Teleflex Medical",
      "address_1": "2917 Weck Dr",
      "address_2": "N/A",
      "postal_code": "27709-0186",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "CA, CT, FL, IL, IN, MD, MI, MN, MO, MS, NC, NJ, NY, NV, OH, PA, TX, VA, WI and WV.",
      "recall_number": "Z-2251-2017",
      "product_description": "Hudson RCI, Pediatric Nasal Cannula, Non-Flared Prongs, Rx only,",
      "product_quantity": "1150 units",
      "reason_for_recall": "Incorrect labeling; the box label indicates \u001cPediatric,\u001d the product insert indicates an \u001cAdult\u001d device.",
      "recall_initiation_date": "20170509",
      "center_classification_date": "20170607",
      "termination_date": "20250116",
      "report_date": "20170614",
      "code_info": "Product Code: 1101, Lot numbers: 74J1603122, 74K1601506, 74K1602306 and 74L16006."
    }
  ]
}